Variant #0000514106 (NC_000002.11:g.211518741C>T, NC_000002.11(NM_001122633.2):c.3499-8C>T (CPS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.211518741C>T
DNA change (hg38) g.210654017C>T
Published as CPS1(NM_001122633.2):c.3499-8C>T (p.(=)), CPS1(NM_001875.4):c.3481-8C>T
ISCN -
DB-ID CPS1_000280 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00467 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPS1 NM_001122633.2 -?/. - c.3499-8C>T r.(=) p.(=)
CPS1 NM_001875.4 -?/. - c.3481-8C>T r.(=) p.(=)


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